õüǰп

  • õüǰпҴ õ Դϴ.
ҽ Ʈ
No. ()
м (ȣ) Page ǿ ũ
45 Jin Sook Lee( ) GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.
Ann Neurol 82(3) 466-478 2017 pubmed
44 Jin Sook Lee() Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center
Muscle Nerve 55(5) 727-734 2017 pubmed
43 Jin Sook Lee( 1) Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathy.
Brain Dev 0387-7604(17) 30140-7 2017 pubmed
42 Jin Sook Lee(1) eIF2B-related multisystem disorder in two sisters with atypical presentations
Eur J Paediatr Neurol 21(2) 404-409 2017 pubmed
41 Jin Sook Lee(1) Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathy.
Brain Dev 39(9) 799-803 2017 pubmed

 10   1 2 3 4 5 6 7 8 9 10  10

ԽùƮ ˻